chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101526566615265667T-13GENIChomozygous51624349
101526617815266179TG12GENIChomozygous51812207
101526622815266229AG9GENIChomozygous51812209
101526628615266287CT14GENIChomozygous51812211
101526633915266342AGG---19GENIChomozygous51812213
101526636715266368AAAG15GENIChomozygous51812215
101526647115266472CA17GENIChomozygous51812217
101526654615266547CT23GENICheterozygous51812219
101526664915266650GA21GENICpossibly homozygous51812221
101526677515266776AAAG12GENIChomozygous51331012
101526677915266780GGAGAGAGAA19GENIChomozygous51624351
101526718815267189GA21GENICheterozygous51624352
101526769615267697T-13GENIChomozygous51624356
101526831515268316CT17GENICpossibly homozygous51812223
101526846515268466CT27GENIChomozygous51812225
101526851515268516AG29GENIChomozygous51624357
101526866915268670A-19GENIChomozygous51812227
101526872915268730TC16GENIChomozygous51812229
101526877415268775AG19GENIChomozygous51812231
101526879915268800CCA13GENICheterozygous51624358
101526922915269230GA27GENIChomozygous51812233
101526949815269499AAT21GENIChomozygous51812235
101526985915269860AAG17GENIChomozygous51812237
101526989215269893TC18GENIChomozygous51812239
101527005515270056AG25GENIChomozygous51812241
101527015315270154GA18GENIChomozygous51812243
101527052415270525T-8GENIChomozygous51812245
101527136215271363GA25GENIChomozygous51812247
101527226215272263GT27GENIChomozygous51812249
101527285915272860CCGATA8GENIChomozygous51331013
101527290015272901GGATAA13GENIChomozygous51331014
101527290015272901GA14GENICheterozygous51812251
101527344215273443GA24GENIChomozygous51812253
101527384715273849TG--17GENIChomozygous51812255